CN1904006B

CN1904006B - Mineral oils with improved conductivity and cold flowability

Info

Publication number: CN1904006B
Application number: CN200610100097.9A
Authority: CN
Inventors: M·克鲁尔; W·赖曼
Original assignee: Clariant Produkte Deutschland GmbH
Current assignee: Clariant Produkte Deutschland GmbH
Priority date: 2005-07-28
Filing date: 2006-06-29
Publication date: 2013-03-27
Anticipated expiration: 2026-06-29
Also published as: EP1749873A2; DE102005035277A1; CA2554168A1; JP2007031715A; US7713315B2; US20070022654A1; CA2554168C; KR101469522B1; RU2006127366A; DE102005035277B4; EP1749873B1; CN1904006A; EP1749873A3; KR20070015086A; RU2419652C2; JP5199554B2

Abstract

A mineral oil distillate having a water content of less than 150 ppm and a conductivity of at least 50 pS/m, comprises 0.1-200 ppm at least one alkylphenolaldehyde resin and 0.1-200 ppm at least one nitrogen-containing polymer.

Description

Mineral oil with improved specific conductivity and cold flowability

Technical field

The present invention relates to alkylphenol-aldehyde resins and polymer with nitrogen for improvement of the purposes of the specific conductivity of low water mineral oil fractions, and relate to the mineral oil fractions that adds additive.

Background technology

In day by day severe environmental legislation process, sulfocompound and the aromatic hydrocarbon content in mineral oil fractions must further descend.But in the refinery processes for the production of the mineral oil quality that meets the specification, other polarity and aromatic substance also are removed simultaneously.At this, oil also often descends to the absorptive capacity of water.As side effect, greatly reduce thus the specific conductivity of these mineral oil fractions.Therefore, as especially under high flow rate, for example in the pipeline in the refinery and the circulation pumping procedure in the strainer, in distribution claim and the static charge that in human consumer's equipment, produces can not be balanced.But the danger of the under cover spark discharge of this potential difference between oil and its surrounding environment, this spark discharge may cause spontaneous combustion or the blast of inflammable liquid.Therefore, can improve specific conductivity and help oil and its surrounding environment between the additive of electric potential balancing add in these oil with low conductivity.Debatable especially at this is the raising of specific conductivity under the low temperature, because the specific conductivity of organic liquid reduces along with drop in temperature and known additive also demonstrates identical temperature dependency.Generally be regarded as being enough to be used in the safety operation of mineral oil fractions greater than the specific conductivity of 50pS/m.Be used for determining that the method for specific conductivity for example is described in DIN 51412-T02-79 and ASTM 2624.

A compounds that uses in mineral oil for various purposes is alkyl phenol resin and its derivative, and it can be by preparing with phenols and aldehyde condensation under acidity or alkaline condition of alkyl group.For example, alkyl phenol resin is used as the cold flow improving agent, lubrication modifier, and oxidation retarder, inhibiter and pitch dispersion agent, and the alkoxylated alkylphenol resin is as the emulsion splitter in crude oil and the middle runnings.In addition, alkyl phenol resin is as the stablizer of jet fuel.Equally, the cold additive that the resin that is generated by benzoic ether and aldehydes or ketones is used as oil fuel.

Another kind of mineral oil additive is polymkeric substance, and they comprise derived from the structural unit of nitrogen containing monomer and can for example be added in the oil fuel to improve various performance such as cold flowability, oilness, and improvement specific conductivity.

EP-A-1 088 045 discloses alkyl phenol resin can be with oil soluble polarity nitrogenous compound for improvement of the low-temperature performance of middle runnings and the oilness of low sulphur fuel oil.

EP-A-1 502 938 discloses the oil fuel with improved specific conductivity, and they can comprise the mixture that is formed by the ester of vinylformic acid, methacrylic acid and the fumaric acid that can optionally comprise the polymer-type of nitrogenous comonomer and following material: polysulfones and the polymer-type reaction product that is generated by Epicholorohydrin and aliphatic series uncle's monoamine or N-alkyl-Alkylenediamine; Or alternative, by the oil-soluble copolymer of alkyl vinyl monomer and cationic vinyl monomer generation.According to the 17th to 19 section, these oil can comprise antioxidant, for example BHT in addition.

EP-A-1 274 819 discloses the oil fuel with improved specific conductivity, and they comprise the oil-soluble copolymer that is generated by alkyl vinyl monomer and cationic vinyl monomer, the mixture that polysulfones and polyamines optionally or its sulfonate form.

EP-A-0 964 052 discloses the multipolymer by ethene and the generation of nitrogenous comonomer of the lubrication modifier that middle runnings is used as low-sulfur.

US-4 356 002 discloses the purposes of oxa alkyl alkyl phenol resin as the static inhibitor of hydrocarbon.Employing by maleic anhydride and alpha-olefin generate with the multipolymer of amino the time, this causes collaborative improved specific conductivity.The preparation of the multifunctional additive for lubricating oils that is formed by this two classes material causes difficulty, because their immiscibles and therefore form heterogeneous system almost.

The specific conductivity improving agent of most of commercial uses comprises metal ion and/or polysulfones as the active substance component.Described polysulfones is by SO ₂Multipolymer with the alkene generation.But becoming the additive of ash and sulfur-bearing is undesirable to being used for low-sulfur fuel in principle.The oil soluble nitrogenous compound that is called other binder component is not enough as the effectiveness self of specific conductivity improving agent, and it is the same according to the combination of US-4 356 002 with the oxa alkyl alkyl phenol resin as these polarity, oil soluble nitrogenous compound, along with the decline of the aromatic substance of the oil of additive to be added and water-content and become more unsatisfactory.But for these oil, add subsequently entry and only cause the dispersion of undissolved water in oil, this is helpless to the improvement of specific conductivity, and is the increase that causes etching problem on the contrary, and under cold condition, there are icing danger and the obstruction of the delivery conduit that causes thus and strainer.

Therefore, the objective of the invention is to find a kind of additive being superior to prior art aspect its effectiveness, it is for improvement of the mineral oil fractions with low water content, especially the specific conductivity of the mineral oil fractions of low aromatic, this additive even also guarantee in addition at low temperatures the safety operation that these are oily.In order not stay resistates when burning, this additive should and especially not comprise any metal without the lacquer putty burning.In addition, it should not conform to halogenide or sulfocompound.

Summary of the invention

Now be surprisingly found out that, the mineral oil of low aromatic can be significantly improved aspect its specific conductivity by adding a small amount of phenol resins (composition I) and polymer with nitrogen (composition II).Specific conductivity is compared the increase that obtains obvious higher degree by the combination of these two kinds of binder components with the effect of the single material of expecting.In addition, specific conductivity keeps constant and raises in many cases even along with the decline of temperature along with the decline of temperature.The oil that so adds additive shows the specific conductivity that greatly increases and therefore can significantly more safely operate especially at low temperatures.

Therefore the present invention provides and comprises at least a purposes that comprises the alkylphenol-aldehyde resins of following formula structural unit and count the composition of 0.1 to 10 at least a polymer with nitrogen of weight part based on these one or more alkylphenol-aldehyde resins,

R wherein ⁵C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, O-R ⁶Or O-C (O)-R ⁶, R ⁶C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, and n is 2 to 100 number, described purposes is the specific conductivity that is lower than the mineral oil fractions of 150ppm for improvement of water-content.

The present invention further provides at least a purposes that comprises the alkylphenol-aldehyde resins (composition I) of following formula structural unit,

R wherein ⁵C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, O-R ⁶Or O-C (O)-R ⁶, R ⁶C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, with n be 2 to 100 number, described purposes is for improvement of having the water-content that is lower than 150ppm and comprise the specific conductivity of the low aromatic mineral oil fractions of 0.1 to 200ppm at least a polymer with nitrogen (composition II), and the consumption of described alkylphenol-aldehyde resins is 50pS/m at least so that mineral oil fractions has specific conductivity.

The present invention further provides a kind of method of specific conductivity that water-content is lower than the mineral oil fractions of 150ppm of improving, it is undertaken by add a kind of composition in this mineral oil fractions, said composition comprises at least a alkylphenol-aldehyde resins that comprises the following formula structural unit

R wherein ⁵C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, O-R ⁶Or O-C (O)-R ⁶, R ⁶C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, and n is 2 to 100 number, and count at least a polymer with nitrogen of 0.1 to 10 weight part based on described alkylphenol-aldehyde resins, so that having specific conductivity, mineral oil fractions is at least 50pS/m.

The present invention further provides a kind of method of specific conductivity that water-content is lower than 150ppm and comprises the mineral oil fractions of 0.1 to 200ppm at least a polymer with nitrogen of improving, it is undertaken by add 0.1 to the 200ppm at least a alkylphenol-aldehyde resins that comprises the following formula structural unit in this mineral oil fractions

R wherein ⁵C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, O-R ⁶Or O-C (O)-R ⁶, R ⁶C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, and n is 2 to 100 number is 50pS/m at least so that mineral oil fractions has specific conductivity.

The present invention further provides water-content and be lower than 150ppm and specific conductivity and be the mineral oil fractions of 50pS/m at least, it comprises 0.1 to the 200ppm at least a alkylphenol-aldehyde resins that comprises the following formula structural unit,

R wherein ⁵C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, O-R ⁶Or O-C (O)-R ⁶, R ⁶C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, and n is 2 to 100 number, and 0.1 to 200ppm at least a polymer with nitrogen.

The present invention further provides the mineral oil fractions additive that water-content is lower than 150ppm, it comprises take at least a alkylphenol-aldehyde resins and at least a polymer with nitrogen of mass ratio as 99: 1 to 1: 99.

Within the scope of the present invention, alkylphenol-aldehyde resins refers to all polymkeric substance that can obtain by the condensation with the phenol of alkyl group and aldehydes or ketones.Alkyl group can directly be bonded to by the C-C key on the aromatic yl group of phenol or be bonded on it by functional group such as ester or ether at this.

Preferred use 0.2 to 100ppm and especially 0.25 to 25ppm, 0.3 to 10ppm at least a alkylphenol-aldehyde resins for example, and 0.2 to 50ppm and especially 0.25 to 25ppm, for example 0.3 to 20ppm at least a polymer with nitrogen is with the improvement specific conductivity.Particularly preferably use altogether to be up to 100ppm preferred 0.2 to 70ppm and especially 0.3 to 50ppm the combination that is formed by one or more alkylphenol-aldehyde resins and one or more polymer with nitrogen.

Mineral oil fractions of the present invention preferably comprises 0.2 to 100ppm and especially 0.25 to 25ppm, 0.3 to 10ppm at least a alkylphenol-aldehyde resins for example, and 0.2 to 50ppm and especially 0.25 to 25ppm, for example 0.3 to 20ppm at least a polymer with nitrogen.Mineral oil fractions of the present invention particularly preferably comprises and altogether is up to 100ppm, preferred 0.2 to 70ppm and especially 0.3 to 50ppm the combination that is formed by one or more alkylphenol-aldehyde resins and one or more polymer with nitrogen.

Preferably use 0.2 to 100ppm and especially 0.25 to 25ppm, 0.3 to 10ppm at least a alkylphenol-aldehyde resins for example, comprise 0.2 to 50ppm and especially 0.25 to 25ppm with improvement, for example the specific conductivity of the mineral oil fractions of 0.3 to 20ppm at least a polymer with nitrogen.

At the additive that is used for mineral oil fractions by the present invention, mass ratio is preferably 50: 1 to 1: 50 between composition I and the composition II, and particularly preferably 10: 1 to 1: 10, for example 4: 1 to 1: 4.

Has preferably at least 60pS/m at improved mineral oil fractions of the present invention aspect its specific conductivity, especially at least the specific conductivity of 75pS/m.

Alkylphenol-aldehyde resins as composition I is known in principle, and for example is described in R

MppChemie Lexikon, the 9th edition, the 1988-92 of Thieme press, the 4th volume, the 3351st page and the last few pages.Those alkylphenol-aldehyde resins according to the suitable induced by alkyl hydroxybenzene that especially has one or two alkyl group derived from ortho position and/or contraposition at the OH group of the present invention.Especially preferred parent material be on aromatic substance with at least two can with the induced by alkyl hydroxybenzene of the hydrogen atom of aldehyde condensation, and monoalkylation phenols especially.Particularly preferably, alkyl group is in the contraposition of phenols OH group.Can be identical or different in the alkylphenol-aldehyde resins of alkyl group (it refers to by with undefined alkyl for composition I generality) in can be used for the method according to this invention, they can be saturated or undersaturated and have and be up to 200, preferred 1-20, especially 4-16, for example 6-12 carbon atom; They just are being preferably, the different and tertiary butyl, just and isopentyl, and just and isohexyl, just and iso-octyl, just with different nonyl, just and isodecyl, just with the Permethyl 99A. base, tetradecyl, hexadecyl, octadecyl, three propenyl, the tetrapropylene base, poly-(propenyl) and poly-(isobutenyl) group.These groups are preferably saturated.In a preferred embodiment, alkyl phenol resin is by using the mixture that is formed by the induced by alkyl hydroxybenzene with different alkyl groups to prepare.For example, based on take mol ratio as 1: 10 to 10: 1 butylphenol and octyl group-, nonyl-and/or the resin of dodecyl phenol be proved to be particularly suitable.

Suitable alkyl phenol resin also can comprise by other phenol analogue, such as Whitfield's ointment, and the structural unit of hydroxy-benzoic acid and its derivative such as ester, acid amides and salt formation, or formed by them.

The aldehyde that is applicable to alkylphenol-aldehyde resins be have 1 to 12 carbon atom those and preferably have those of 1 to 4 carbon atom, formaldehyde for example, acetaldehyde, propionic aldehyde, butyraldehyde, 2-ethyl hexanal, phenyl aldehyde, oxoethanoic acid, and its reactive equivalent such as paraformaldehyde and three

Alkane.Particularly preferably be the formaldehyde of paraformaldehyde form and especially formalin.

Utilize the molecular weight of the alkylphenol-aldehyde resins that gel permeation chromatography measures with respect to the PEG standard substance in THF to be preferably 400-20 000g/mol, especially 800-10 000g/mol and particularly 2000-5000g/mol.Prerequisite at this is that alkylphenol-aldehyde resins is oil-soluble under the concentration relevant with application of 0.001 to 1 % by weight at least.

In a preferred embodiment of the invention, described alkyl resinox is to comprise oligopolymer with following formula repeated structural unit or this resinoid of polymkeric substance

R wherein ⁵C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, O-R ⁶Or O-C (O)-R ⁶, R ⁶C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, and n is 2 to 100 number.R ⁶Be preferably C ₁-C ₂₀-alkyl or C ₂-C ₂₀-alkenyl and especially C ₄-C ₁₆-alkyl or C ₂-C ₂₀-alkenyl, for example C ₆-C ₁₂-alkyl or-alkenyl.Particularly preferably, R ⁵C ₁-C ₂₀-alkyl or-alkenyl and especially C ₄-C ₁₆-alkyl or-alkenyl, for example C ₆-C ₁₂-alkyl or-alkenyl.N is preferably 2 to 50 number and especially 3 to 25 number, for example 5 to 15 number.

In order to be used for middle runnings such as diesel oil and oil fuel, particularly preferably be the C with alkylphenol ₂-C ₄₀-alkyl group preferably has C ₄-C ₂₀-alkyl group, for example C ₆-C ₁₂The alkylphenol-aldehyde resins of-alkyl group.Alkyl group can be linearity or branching, and they are preferably linear.Especially suitable alkylphenol-aldehyde resins is derived from the induced by alkyl hydroxybenzene of the linear alkyl group with 8 and 9 carbon atoms.The molecular-weight average that utilizes GPC to measure is preferably 700 to 20 000g/mol, 1000 to 10 000g/mol especially, and for example 2000 to 3500g/mol.

In order to be used for gasoline and jet fuel, particularly preferably be its alkyl group with 4 to 200 carbon atoms, preferred 10 to 180 carbon atoms and derived from oligopolymer or the polymkeric substance of the alkene with 2 to 6 carbon atoms, for example alkylphenol-aldehyde resins of derivative autohemagglutination (iso-butylene).Therefore they are branching preferably.The polymerization degree (n) is preferably 2 to 20 at this, particularly preferably 3 to 10 alkylphenol unit.

These alkylphenol-aldehyde resins can be by known method, for example by corresponding induced by alkyl hydroxybenzene and formaldehyde, namely with 0.5 to 1.5mol, the condensation reaction of preferred 0.8 to 1.2mol formaldehyde/mole alkylphenol and obtaining.Condensation reaction can solvent-freely be carried out, but but but it preferably at non-water compatibility or only inert organic solvents such as the mineral oil of part water compatibility, alcohol carries out under the existence of ether and analogue.Particularly preferably be the solvent that can form with water azeotrope.The such solvent that uses is aromatic substance such as toluene especially, dimethylbenzene, and the commercially available solvent mixture of diethylbenzene and higher, for example

Shellsol AB, and solvent naphtha.Condensation reaction is preferably at 70 to 200 ℃, for example carries out under 90 to 160 ℃.It is usually by 0.05 to 5 % by weight alkali or preferably by 0.05 to 5 % by weight acid catalysis.Except carboxylic acid such as acetic acid and oxalic acid, as an acidic catalyst, strong inorganic acid example hydrochloric acid especially, phosphoric acid, and sulfuric acid, and sulfonic acid is the catalyzer of commonly using.Especially suitable catalyzer is to comprise at least one sulfonic acid group to have 1 to 40 carbon atom and preferably have the saturated or unsaturated of 3 to 24 carbon atoms with at least one, the sulfonic acid of linearity, branching and/or cyclic hydrocarbon group.Particularly preferably be aromatic sulfonic acid, especially have one or more C ₁-C ₂₈The alkyl aromatic list sulfonic acid of-alkyl group and especially have C ₃-C ₂₂Those of-alkyl group.Suitable example is methylsulfonic acid, fourth sulfonic acid, Phenylsulfonic acid, tosic acid, xylene monosulfonic acid, 2-sym-toluenesulfonic acid, 4-ethyl phenenyl azochlorosulfonate acid, isopropyl benzene sulfonic acid, 4-butylbenzene sulfonic acid, 4-octyl group Phenylsulfonic acid; Witco 1298 Soft Acid, two (dodecyl) Phenylsulfonic acid, naphthene sulfonic acid.The mixture of these sulfonic acid also is suitable.Usually, their former states after reaction finishes are retained in the product or to be neutralized form and are retained in the product; Comprise metal ion and common separated the removing of the salt that therefore becomes ash.

Especially suitable polymer with nitrogen is:

A) comprise derived from having C ₄-to C ₄₀The comb-shaped polymer of the monomer of-alkyl group and the unit of at least a nitrogenous comonomer,

B) multipolymer of ethene and the unsaturated nitrogenous comonomer of olefinic, and

C) the polymer-type polyamines that aliphatic series uncle's monoamine or N-alkylenediamines and Epicholorohydrin or Racemic glycidol condensation is prepared.

The applicable composition IIa that does) comb-shaped polymer is especially derived from C ₄-to C ₄₀The ester of the oil soluble ethylenically unsaturated carboxylic acids of-alkyl group, oil-soluble ethylene base ester and/or oil-soluble ethylene base ether.Especially suitable polymkeric substance is poly-(acrylate), poly-(methacrylic ester), poly-(maleic acid ester) and gather (fumarate), it is derived from by vinylformic acid, methacrylic acid, toxilic acid and/or fumaric acid and C ₄-C ₄₀-pure and mild especially with C ₆-to C ₂₂The ester that-alcohol forms.Alkyl group is linearity or branching preferably; They are preferably saturated.For example can mention n-butyl acrylate, ethyl acrylate, vinylformic acid Lauryl Ester, stearyl acrylate base ester, methacrylic acid n-butyl, methacrylic acid-2-ethylhexyl, methacrylic acid Lauryl Ester, methacrylic acid stearyl and analogue.

Another kind of suitable comb-shaped polymer IIa) derived from the alkene with 6 to 42 carbon atoms.Alkene is preferably linear.Two keys are preferably the two keys in end position, for example, at the 1-decane, 1-dodecane, the 1-tetradecane, the end position of 1-n-Hexadecane.Equally preferably by at C ₂₀-C ₂₄, C ₂₂-C ₂₈And C ₂₄-C ₃₀The mixture that various alkene in the chain length scope forms.

Comb-shaped polymer IIa) comprise at least a nitrogenous comonomer, its nitrogen is preferably with amino, amido, and the form of imino-or ammonium group exists and is bonded on the main polymer chain by hydrocarbyl group.They are preferably the C that is interrupted by ester or amide group by can be optionally ₂-to C ₁₂-alkylidene group is bonded to amino or the ammonium group on the main polymer chain.Ammonium group preferably includes by primary, secondary and tertiary amine and mineral acid, organic sulfonic acid and salt preferred and that carboxylic acid forms.Comonomer with quaternary ammonium group also is suitable.

The example of suitable comonomer is the unsaturated basic amine of polymerizable, such as allyl amine and diallyl amine, alkene with amino, as to (2-diethyllaminoethyl) vinylbenzene, nitrogen heterocyclic ring with exocyclic double bond, such as vinyl pyridine and vinyl pyrrolidone, the ester that is formed by ethylenically unsaturated carboxylic acids and amino alcohol, such as vinylformic acid-N, N-(dimethylamino) ethyl ester, methacrylic acid-N, N-(dimethylamino) ethyl ester or methacrylic acid-N, N-(dimethylamino) propyl ester, the acid amides that is formed by diamines and ethylenically unsaturated carboxylic acids, such as N, N-(dimethylamino) propyl methyl acid amides, N-(aminopropyl) morpholine and its quaternary ammonium derivative, such as methacrylic acid-N, N, N-(trimethyl ammonium) ethyl ester Methylsulfate (methosulfate), methacrylic acid-N, N, N-(trimethyl ammonium) propyl ester Methylsulfate, and by ethylenically unsaturated dicarboxylic and the polyamines that comprises wherein 2 to 5 nitrogen-atoms that preferred only form with the primary amino group exists, such as N, the imide that the N-dimethylamino propylamine forms.Particularly preferably be by methacrylic acid-C ₈-C ₁₄-alkyl ester and N, N-(dimethylamino) propyl methyl acid amides or methacrylic acid-N, the polymkeric substance that N-(dimethylamino) propyl ester forms, and by vinylformic acid-C ₈-C ₁₄-alkyl ester and N, N, the multipolymer of N-(trimethyl ammonium) propyl methyl acid amides methylsulfuric acid salt formation.Same suitable be monomer such as vinyl cyanide and methacrylonitrile with nitrile group.

The ester of ethylenically unsaturated carboxylic acids, vinyl ester, vinyl ether and/or alkene are preferably 20: 1 to 1: 1, for example 10: 1 to 3: 1 as a side and nitrogenous comonomer as the opposing party's mol ratio between the two.It is 0.3 to 5 % by weight that these multipolymers preferably have nitrogen content, for example 0.5 to 3 % by weight.

Comb-shaped polymer IIa also can comprise and is up to 20mol%, other comonomer of 1 to 10mol% for example, as have the alpha-olefin of 4 to 40 carbon atoms, acrylamide, Methacrylamide, C ₁-C ₂₀-alkyl acrylamide and/or C ₁-C ₂₀-alkyl methyl acrylamide.

Comb-shaped polymer has preferably that to utilize gel permeation chromatography be 1000 to 100 000g/mol with respect to the molecular weight (Mn) that poly-(vinylbenzene) standard substance is measured in THF, preferred 5000 to 50 000g/mol.

Comb-shaped polymer IIa) preferably the direct copolyreaction by comonomer prepares.But their alternatives also can be by by with C ₁-to C ₄₀The ester of the ethylenically unsaturated carboxylic acids of-alkyl group, vinyl ester, vinyl ether and/or alkene, and the polymer phase that carries out of ethylenically unsaturated carboxylic acids or its reactive derivatives such as acid anhydrides, carboxylic acid halides or the multipolymer that generates with ester that the lower alcohol with 1 to 4 carbon atom forms and oxyamine or polyamines reacts and prepares like changing (polymeranaloge).Suitable oxyamine is, for example, and N, N-dimethylaminoethanol and N-coconut oil fat alkylamino ethanol.Suitable polyamines is, for example, and N, N-dimethylamino propylamine, N-coconut oil fat alkyl propylene diamine and N-butter fatty alkyl propylene diamine.Another preparation method's change programme is that nitrogenous comonomer is grafted to by with C ₁-to C ₄₀On the polymkeric substance that the ester of the ethylenically unsaturated carboxylic acids of-alkyl group, vinyl ester, vinyl ether and/or alkene form.

Polymkeric substance with quaternary ammonium group can be by the copolyreaction of polymerizable quaternary ammonium compound or by preparing like transformation reaction with the polymkeric substance of amino and the polymer phase of alkylating agent such as alkylogen or sulfuric ester.Particularly preferably be the alkylating agent of halogen, for example methyl-sulfate.

Especially preferred polymer with nitrogen IIa) example is methacrylic acid-N, N, N, the multipolymer of-(trimethyl ammonium) ethyl ester Methylsulfate and ethyl acrylate, the multipolymer of lauryl methacrylate and dimethylaminopropyl Methacrylamide, and the alternating copolymer of tetradecene and vinyl cyanide.

Described as polymkeric substance IIb of the present invention) in the unsaturated nitrogenous comonomer of this olefinic of composition except ethene preferably also be applicable to prepare comb-shaped polymer IIa) and comprise by hydrocarbyl group and be bonded to the monomer with the nitrogen of amino, amido, acylimino or ammonium group form on the main polymer chain.For example can mention:

I) alkyl amido acrylate or alkylamino methacrylic ester, acrylic-amino ethyl ester for example, acrylic-amino propyl ester, the positive butyl ester of acrylic-amino, vinylformic acid-N-methylamino ethyl ester, vinylformic acid-N, the N-dimethylamino ethyl ester, vinylformic acid-N, N-(dimethylamino) propyl ester, vinylformic acid-N, N-(diethylamino) propyl ester, vinylformic acid-N, N, N-(trimethyl ammonium) ethyl ester Methylsulfate and corresponding methacrylic ester

Ii) alkyl acrylamide and alkyl methyl acrylamide such as ethyl acrylamide; the butyl acrylamide; the N-octyl acrylamide; the N-propyl group; N-methoxyl group propylene acid amides, N-acryl phthalic imidine, N-acryl succinimide; N hydroxymethyl acrylamide and corresponding Methacrylamide

Iii) vinylamide N-vinyl-N-methylacetamide for example, N-vinyl succinimide,

Iv) aminoalkyl group vinyl ether aminopropyl vinyl ether for example, the diethylamino ethyl vinyl ether, the dimethylaminopropyl vinyl ether,

V) olefinic unsaturated amine such as allyl amine, diallyl amine, N-allyl group-N-methylamine, and N-allyl group-N-ethylamine,

Vi) with the heterocycle of vinyl groups, NVP for example, methyl ethylene imidazoles, 2-vinyl pyridine, 4-vinylpridine, 2-methyl-5-vinylpyrine, vinylcarbazole, vinyl imidazole, N-vinyl-2-piperidone, N-caprolactam.

Preferred multipolymer IIb) comprise, except ethene, 0.1 to 15mol%, especially one or more nitrogenous comonomers of 1 to 10mol%.In addition, they also can comprise other, for example a kind of, two or three other olefinic unsaturated comonomer.Other suitable comonomer is, for example, and vinyl ester, vinylformic acid, methacrylic acid, acrylate, methacrylic ester, vinyl ether and alkene.Especially preferred vinyl ester is vinyl-acetic ester, propionate, vinyl butyrate, sad vinyl acetate, 2 ethyl hexanoic acid vinyl ester, vinyl laurate and the vinyl ester with new carboxylic acid of 8,9,10,11 or 12 carbon atoms.Especially preferred acrylate and methacrylic ester especially have the alcohol of 1 to 4 carbon atom derived from having 1 to 20 carbon atom, such as methyl alcohol, and ethanol and propyl alcohol.Especially preferred alkene is to have those of 3 to 10 carbon atoms, propylene especially, butylene, iso-butylene, diisobutylene, 4-methylpentene, hexene and norbornylene.If multipolymer IIb) comprise another kind of comonomer, then its molar ratio is preferably and is up to 15mol%, and especially 1 to 12mol%, and for example 2 to 10mol%.

Melt viscosity at 140 ℃ of lower these multipolymers of measuring preferably is lower than 10 000mPas, and especially 10 to 1000mPas, for example 20 to 500mPas.

Comonomer by known method (to this referring to, for example, Ullmanns Encyclop Dieder Technischen Chemie (the Liv Ullmann technical chemistry is complete works of), the 4th edition, the 19th volume, the 169th to 178 page) and copolymerization.Suitable is in solution, in suspension, and the polyreaction in gas phase and high pressure bulk polymerization.Preferred to use at pressure be 50 to 400MPa, and preferred 100 to 300MPa, and temperature is 50 to 350 ℃, the high pressure bulk polymerization that carries out under preferred 100 to 300 ℃.The reaction of comonomer causes by the initiator (free radical chain initiator) that can form free radical.This material classification comprises, for example, and oxygen, hydroperoxide, superoxide and azo-compound, such as cumene hydroperoxide, t-butyl hydroperoxide, dilauroyl peroxide, dibenzoyl peroxide, di（2-ethylhexyl peroxy） dicarbonate, cross the toxilic acid tertiary butyl ester, t-butyl perbenzoate, dicumyl peroxide, the tert-butyl peroxide cumyl, two (tertiary butyl) superoxide, 2,2 '-azo two (2-methyl propionitrile), 2,2 '-azo two (2-methylbutyronitrile).Initiator separately or as the form of mixtures that is formed by two or more materials to count 0.01 to 20 % by weight based on copolymerized monomer mixture, the amount use of preferred 0.05 to 10 % by weight.For the composition of given copolymerized monomer mixture, the required melt viscosity of multipolymer and therefore molecular weight by changing reaction parameter, pressure and temperature, and optionally regulating by adding negative catalyst.Verified for suitable negative catalyst is hydrogen, saturated or unsaturated hydrocarbons, propane for example, propylene, aldehyde, such as propionic aldehyde, butyraldehyde-n or isobutyric aldehyde, ketone, such as acetone, methyl ethyl ketone, methyl iso-butyl ketone (MIBK), pimelinketone, or alcohol are such as butanols.Depend on the viscosity of making every effort to, negative catalyst is to be up to 20 % by weight based on copolymerized monomer mixture, and the amount of preferred 0.05 to 10 % by weight is used.

The high pressure bulk polymerization for example carries out in autoclave or the tubular reactor intermittently or continuously at known high-pressure reactor; It is especially applicable that tubular reactor has been proved to be.Solvent such as aliphatic hydrocrbon or hydrocarbon mixture, benzene or toluene can be present in the reaction mixture, but solvent-free operating method has been proved to be especially applicable.By the preferred embodiment of polyreaction, by comonomer, initiator and, if use, the mixture that negative catalyst forms is fed in the tubular reactor by reactor inlet with by one or more side branch.Can have different composition (EP-B-0 271 738 and EP-A-0 922 716) in this comonomer logistics.

According to the same suitable multipolymer IIb of the present invention) ethylene copolymer that can be by will comprising acid groups prepares with the compound reaction with amino group.The ethylene copolymer and the ethylene-dien terpolymer that are applicable to this are for example, to comprise vinylformic acid, methacrylic acid, methylene-succinic acid, fumaric acid, those of toxilic acid or maleic anhydride.In order to prepare multipolymer IIb of the present invention), with these multipolymers that contain acid groups by acid groups and alkanolamine such as thanomin, Propanolamine, diethanolamine, the N-ehtylethanolamine, N, N-dimethylethanolamine, diglycolamine, 2-amino-2-methyl Propanolamine and/or polyamines such as quadrol and dimethylamino propylamine and/or N-alkyl alkylene polyamine such as N-coconut oil fat alkyl trimethylene diamine or corresponding compound or its mixture reaction with ammonium group.Every equimolar acid uses 0.1 to 1.2mol, the amine of preferred equimolar amount.

Can be converted to quaternary ammonium salt by the direct polymerization reaction with by polymer phase by the reaction with alkylating agent such as alkylogen or sulfuric ester like the nitrogenous ethylene copolymer that transformation reaction prepares.Particularly preferably be the alkylating agent of halogen, for example methyl-sulfate at this.

According to the applicable composition IIc that does of the present invention) the polymer-type polyamines refer in particular to and in molecule, have 4 or more, preferred 6 or more, for example 8 or the polyamines of more nitrogen-atoms.Nitrogen-atoms is the integral part of main chain at this.Main polymer chain is preferably with having 8 and the alkyl group side chain of more carbon atoms.

The polymer-type polyamines is preferably the condensation product that was generated in 1: 1 to 1: 1.5 according to mol ratio by amine and Epicholorohydrin or Racemic glycidol.Preferably based on uncle's monoamine, alkylamine especially, and based on the polymkeric substance of N-alkylenediamines, its alkyl group have 8 to 24 and especially 8 to 12 carbon atoms have 2 to 6 carbon atoms with its alkylidene group, N-alkyl-1 for example, 3-propylene diamine.Alkyl group is preferably linear.Condensation product IIc) preferably having the polymerization degree is 2 to 20.

The polymer with nitrogen IIa that exists as alkaline amino group of nitrogen wherein), IIb) and IIc) preferably with the form of salt with especially with the form use of sulfonate.The preferred sulfonic acid that is used for salt formation is oil-soluble sulfonic acid such as alkane sulfonic acid, aryl sulfonic acid and alkyl aryl sulphonic acid, for example Witco 1298 Soft Acid.

For more simply operation, the present composition preferably uses with the enriched material form that comprises 10 to 90 % by weight and preferred 20 to 60 % by weight solvents.Preferred solvent is the aliphatic hydrocrbon of higher, aromatic hydrocarbon, alcohol, ester, ether, and its mixture.In enriched material, can change according to applicable cases as the alkylphenol-aldehyde resins of the present invention of composition I with as the mixture ratio between the nitrogenous compound of composition II.Such enriched material preferably comprises 0.1 to 10 weight part, the polar oil-soluble nitrogenous compound of preferred 0.2 to 6 weight part/weight part alkylphenol-aldehyde resins.

In order further to increase the specific conductivity of mineral oil, additive of the present invention also can be used in combination with polysulfones.Suitable polysulfones can by sulfurous gas with have the 1-alkene of 6 to 20 carbon atoms, for example copolyreaction of 1-dodecylene and obtaining.They have the molecular weight that utilizes GPC to measure with respect to poly-(vinylbenzene) standard substance is 10 000 to 1 500 000, preferred 50 000 to 900 000 and especially 100 000 to 500 000.The preparation example of suitable polysulfones is as learning from US 3 917 466.

Additive of the present invention can be added in the mineral oil fractions to improve cold flowability, simultaneously also with other additive, ethylene copolymer for example, paraffin dispersant, comb-shaped polymer, poly (oxyalkylene) based compound and/or olefin copolymer combine.

In a preferred embodiment, the present invention's additive of being used for mineral oil fractions also comprises one or more of composition III to VII except comprising composition I and II.

For example, they preferably comprise the multipolymer that formed by ethene and alefinically unsaturated compounds as composition III.Suitable ethylene copolymer especially also comprises 6 to 21mol% except ethene, especially those of 10 to 18mol% comonomers.

Alefinically unsaturated compounds preferably refers to vinyl ester, acrylate, and methacrylic ester, alkyl vinyl ether and/or alkene, wherein mentioned compound can be replaced by oh group.One or more comonomers can be present in the polymkeric substance.Vinyl ester preferably refers to those of formula 1

CH ₂＝CH-OCOR ¹ (1)

R wherein ¹C ₁-to C ₃₀-alkyl, preferred C ₄-to C ₁₆-alkyl, especially C ₆-to C ₁₂-alkyl.In another embodiment, mentioned alkyl group can be replaced by one or more oh groups.

In a further preferred embodiment, R ¹Be to have 7 to 11 carbon atoms, especially have branched-alkyl group or the new alkyl group of 8,9 or 10 carbon atoms.Especially preferred vinyl ester is in secondary carboxylic ester and the tertiary carboxylic acid especially of the alpha-position of carbonyl group derived from its side chain.Suitable vinyl ester comprises vinyl-acetic ester, propionate, vinyl butyrate, the isopropylformic acid vinyl acetate, vinyl caproate, enanthic acid vinyl acetate, sad vinyl acetate, new vinyl acetate acid, 2-ethyl-caproic acid vinyl ester, vinyl laurate, stearic acid vinyl ester and Versatic acid (branched paraffin carboxylic acid) ester, such as new n-nonanoic acid vinyl acetate, vinyl neodecanoate, new undecanoic acid vinyl acetate.

In other preferred embodiment, these ethylene copolymers comprise vinyl-acetic ester and at least a other the vinyl ester of formula 1, wherein R ¹C ₄-to C ₃₀-alkyl, preferred C ₄-to C ₁₆-alkyl, especially C ₆-to C ₁₂-alkyl.

Acrylate is preferably those of formula 2

CH ₂＝CR ²-COOR ³ (2)

R wherein ²Hydrogen or methyl, and R ³C ₁-to C ₃₀-alkyl, preferred C ₄-to C ₁₆-alkyl, especially C ₆-to C ₁₂-alkyl.Suitable acrylate comprises, for example, (methyl) methyl acrylate, (methyl) ethyl propenoate, (methyl) propyl acrylate, (methyl) n-butyl acrylate and isobutyl ester, (methyl) Ethyl acrylate, monooctyl ester, 2-ethylhexyl, the last of the ten Heavenly stems ester, dodecyl ester, tetradecyl ester, cetyl ester, stearyl, and the mixture of these comonomers.In another embodiment, mentioned alkyl group can be replaced by one or more oh groups.An example of such acrylate is the methacrylic acid hydroxyethyl ester.

Alkyl vinyl ether preferably refers to the compound of formula 3

CH ₂＝CH-OR ⁴ (3)

R wherein ⁴C ₁-to C ₃₀-alkyl, preferred C ₄-to C ₁₆-alkyl, especially C ₆-to C ₁₂-alkyl.For example can mention methylvinylether, ethyl vinyl ether, IVE.In another embodiment, mentioned alkyl group can be replaced by one or more oh groups.

Alkene preferably refers to have 3 to 30 carbon atoms, especially 4 to 16 carbon atoms and especially the cholesterol hydrocarbon of 5 to 12 carbon atoms.Suitable alkene comprises propylene, butylene, iso-butylene, amylene, hexene, 4-methylpentene, octene, diisobutylene and norbornylene and its derivative such as methyl norbornylene and vinyl norbornene.In another embodiment, mentioned alkyl group can be replaced by one or more oh groups.

Particularly preferably be and except ethene, also comprise 3.5 to 20mol%, especially 8 to 15mol% vinyl-acetic esters, with 0.1 to 12mol%, especially 0.2 to 5mol% is at least a than long-chain and vinyl ester preferred branched, 2 ethyl hexanoic acid vinyl ester for example, the terpolymer of new n-nonanoic acid vinyl acetate or vinyl neodecanoate, wherein total copolymerization monomer content is 8 to 21mol%, preferred 12 to 18mol%.Except ethene and 8 to 18mol% vinyl ester, further especially preferred multipolymer also comprises 0.5 to 10mol% alkene, such as propylene, and butylene, iso-butylene, hexene, 4-methylpentene, octene, diisobutylene and/or norbornylene.

The melt viscosity that these ethylene copolymers and terpolymer preferably have under 140 ℃ is 20 to 10 000mPas, and especially 30 to 5000mPas, and especially 50 to 2000mPas.Utilize ¹The spectrometric degree of branching of H-NMR is preferably 1 to 9 CH ₃/ 100 CH ₂Group, especially 2 to 6 CH ₃/ 100 CH ₂Group, described group are not to be derived from comonomer.

The preferred mixture that is formed by two or more above-mentioned ethylene copolymers that uses.Particularly preferably, the base polymer of this mixture is different at least a characteristic.For example, they can comprise different comonomers, have different co-monomer content, molecular weight and/or the degree of branching.

Additive of the present invention and can change in grace period according to applicable cases as the mixture ratio between the ethylene copolymer of composition III, wherein said ethylene copolymer III often accounts for larger proportion.Such additive agent mixture preferably comprises 2 to 70 % by weight, the additive combination of the present invention that is comprised of I and II of preferred 5 to 50 % by weight, and 30 to 98 % by weight, the ethylene copolymer of preferred 50 to 95 % by weight.

Preferably refer to by the reaction product of aliphatic amide with the compound generation that comprises at least one carboxyl groups according to the applicable paraffin dispersant (composition IV) of making further component of the present invention.Preferred amine refers to formula NR ⁶R ⁷R ⁸Compound, R wherein ⁶, R ⁷And R ⁸Can be identical or different, and at least one be C in these groups ₈-C ₃₆-alkyl, C ₆-C ₃₆-cycloalkyl, C ₈-C ₃₆-alkenyl, especially C ₁₂-C ₂₄-alkyl, C ₁₂-C ₂₄-alkenyl or cyclohexyl, and all the other groups are hydrogen, C ₁-C ₃₆-alkyl, C ₂-C ₃₆-alkenyl, cyclohexyl, or formula-(A-O) _x-E or-(CH ₂) _nThe group of-NYZ, wherein A is ethyl or propyl group, x is 1 to 50 number, E=H, C ₁-C ₃₀-alkyl, C ₅-C ₁₂-cycloalkyl or C ₆-C ₃₀-aryl, and n=2,3 or 4, and Y and Z be H independently of one another, C ₁-C ₃₀-alkyl or-(A-O) _xBut alkyl and kiki alkenyl group linearity or branching and comprise and be up to two two keys.They are preferably linear and basically saturated, and namely they have the 75g of being lower than I ₂/ g preferably is lower than 60g I ₂/ g and especially 1 to 10g I ₂The iodine number of/g.Particularly preferably be secondary aliphatic amide, wherein R ⁶, R ⁷And R ⁸Two in the group is C ₈-C ₃₆-alkyl, C ₆-C ₃₆-cycloalkyl, C ₈-C ₃₆-alkenyl, especially C ₁₂-C ₂₄-alkyl, C ₁₂-C ₂₄-alkenyl or cyclohexyl.Suitable aliphatic amide is, for example, and octylame, decyl amine, lauryl amine, tetradecylamine, hexadecylamine, octadecylamine, eicosyl amine, docosyl amine, didecylamine, two (dodecyl) amine, two (tetradecyl) amine, two (hexadecyl) amine, two (octadecyl) amine, two (eicosyl) amine, two (docosyl) amine, and its mixture.Amine especially comprises the chain fragment based on natural matter, coconut oil fat amine for example, tallow amine, hydrogenated tallow amine, two coconut oil fat amine, two tallow amines and two (hydrogenated tallow amine).Particularly preferred sulfonamide derivatives is amine salt, imide and/or acid amides, and for example by secondary aliphatic amide, acid amides-ammonium salt of generating of two coconut oil fat amine, two tallow amines and distearyl amine especially.Especially preferred paraffin dispersant as composition II comprises the carboxyl groups that at least one is converted to ammonium salt.They especially comprise at least two, and for example at least three or at least four, and in the situation that the polymer-type paraffin dispersant, even five and more ammonium groups.

Carboxyl groups refers to the functional group of following formula at this:

＞C＝O

The carbonyl compound that is suitable for reacting with amine is haplotype and the two kinds of compounds of polymer-type with one or more carboxylic groups.Preferred haplotype carbonyl compound is to have those of 2,3 or 4 carbonyl groups.They also can comprise heteroatoms such as oxygen, sulphur and nitrogen.Suitable carboxylic acid is, for example, and toxilic acid, fumaric acid, β-crotonic acid, methylene-succinic acid, succsinic acid, C ₁-C ₄₀-alkenyl succinic, hexanodioic acid, pentanedioic acid, sebacic acid and propanedioic acid, and phenylformic acid, phthalic acid, TMLA and pyromellitic acid, nitrilotriacetic acid(NTA), ethylenediamine tetraacetic acid (EDTA) and its reactive derivatives, for example ester, acid anhydrides and carboxylic acid halides.The polymer-type carbonyl compound that has confirmed to be suitable for is especially by ethylenic unsaturated acid, vinylformic acid for example, methacrylic acid, toxilic acid, the multipolymer that fumaric acid and methylene-succinic acid generate; Particularly preferably be the multipolymer that is generated by maleic anhydride.Suitable comonomer be to multipolymer give oil-soluble those.Oil soluble refers at this, with the aliphatic amide reaction after, this multipolymer do not have resistates ground with the metering relevant with reality than in the mineral oil fractions that is dissolved in additive to be added.Suitable comonomer is, for example, alkene has 2 to 75 in alkyl group, preferred 4 to 40 and the especially vinylformic acid of 8 to 20 carbon atoms and alkyl ester, alkyl vinyl ester and the alkyl vinyl ether of methacrylic acid.In the situation that alkene, carbon number is based on the alkyl group that is keyed on two keys.Especially suitable comonomer is the alkene with terminal double link.The molecular weight of polymer-type carbonyl compound is preferably 400 to 20000, and particularly preferably 500 to 10 000, for example 1000 to 5000.

What confirmed particularly suitable is by aliphatic series or aromatic amine, preferred long chain aliphatic amine, with aliphatic series or aromatics list-, two, three-or the reaction of tetracarboxylic acid or its acid anhydrides and the paraffin dispersant (referring to US 4 211 534) that obtains.It is same applicable that what make paraffin dispersant is by amino alkylidenyl poly carboxylic acid such as nitrilotriacetic acid(NTA) or ethylenediamine tetraacetic acid (EDTA) acid amides and the ammonium salt (referring to EP 0 398 101) with the secondary amine generation.Other paraffin dispersant is by maleic anhydride and can be optionally and the α of uncle's monoalkylamine and/or fatty alcohol reaction, the multipolymer that β-unsaturated compound generates is (referring to EP-A-0154 177, EP 0 777 712), the reaction product of alkenyl-spirodilactone and amine (referring to EP-A-0413 279 B1), with according to EP-A-0 606 055 A2, based on α, β-unsaturated dicarboxylic acid acid anhydride, α, β-unsaturated compound, and the reaction product of the terpolymer of the polyoxy alkylidene ether of rudimentary unsaturated alcohol.

Additive of the present invention and can change according to applicable cases as the mixture ratio between the paraffin dispersant of composition IV.Such additive agent mixture preferably comprises 10 to 90 % by weight, the additive combination of the present invention that is comprised of I and II of preferred 20 to 80 % by weight, and 10 to 90 % by weight, the paraffin dispersant of preferred 20 to 80 % by weight.

Suitable comb-shaped polymer (composition V) can for example be described by following formula

In the formula

A is R ', COOR ', OCOR ', R " COOR ', OR ';

D is H, CH ₃, A or R ";

E is H, A;

G is H, R ", R " COOR ', aromatic yl group or heterocyclic group;

M is H, COOR ", OCOR ", OR " and, COOH;

N is H, R ", COOR ", OCOR, aromatic yl group;

R ' is the hydrocarbon chain with 8 to 50 carbon atoms;

R " is the hydrocarbon chain with 1 to 10 carbon atom;

M is 0.4 to 1.0 number; With

N is 0 to 0.6 number.

Suitable comb-shaped polymer is, for example by ethylenically unsaturated dicarboxylic such as toxilic acid or fumaric acid, and with other ethylenically unsaturated monomer such as alkene or vinyl ester, the multipolymer that generates of vinyl-acetic ester for example.The alpha-olefin with 10 to 24 carbon atoms at this especially suitable alkene, 1-decene for example, 1-dodecylene, tetradecene, cetene, 1-vaccenic acid, and its mixture.Also be suitable for and make the oligomeric C of being based on of comonomer ₂-C ₆-alkene than long-chain olefin, for example have poly-(iso-butylene) of a high proportion of terminal double link.Usually, these multipolymers adopt the pure esterification at least 50% with 10 to 22 carbon atoms.Suitable alcohol comprises positive decen-1-ol, n-dodecane-1-alcohol, n-tetradecane-1-alcohol, n-hexadecane-1-alcohol, Octadecane-1-alcohol, pure and mild its mixture of NSC 62789-1-.Particularly preferably be the mixture by the pure and mild n-hexadecane of n-tetradecane-1--1-alcohol forms.It is same applicable that what make comb-shaped polymer is poly-(alkyl acrylate) derived from the alcohol with 12 to 20 carbon atoms, poly-(alkyl methacrylate) and poly-(alkyl vinyl ether), and derived from gather (vinyl ester) of the lipid acid with 12 to 20 carbon atoms.

The applicable poly (oxyalkylene) based compound (composition VI) of making other component is, for example, has ester, ether and the ether/ester of polyvalent alcohol of the alkyl group of 12 to 30 carbon atoms with at least one.If alkyl group is derived from acid, all the other are derived from polyvalent alcohol so; If alkyl group is from Fatty Alcohol(C12-C14 and C12-C18), the rest part of this compound is derived from polyacid so.

Suitable polyvalent alcohol is that to have molecular weight be approximately 100 to approximately 5000, preferred 200 to 2000 polyoxyethylene glycol, polypropylene glycol, polytetramethylene glycol and its multipolymer.Also suitable is the alcoxylates of polyvalent alcohol, for example glycerine, TriMethylolPropane(TMP), tetramethylolmethane, neopentyl glycol and can be from its oligopolymer with 2 to 10 monomeric units that obtains by condensation, for example alcoxylates of Polyglycerine.Preferred alcoxylates is to have 1 to 100mol, 5 to 50mol ethylene oxides especially, those of propylene oxide and/or oxybutylene/mole polyvalent alcohol.Ester is especially preferred.

Lipid acid with 12 to 26 carbon atoms is preferred for forming ester additive with polyol reaction, wherein particularly preferably uses C ₁₈-to C ₂₄-lipid acid, especially stearic acid is with docosoic.Ester also can prepare by the esterification polyoxyalkylated alcohols.Preferably having molecular weight is 150 to 2000, the polyoxyalkylated polyvalent alcohol of preferred 200 to 600 complete esterification.Especially suitable is PEG-600-Er docosoic ester and glycerine-ethylene glycol-San docosoic esters.

Suitable conduct can directly belong to unsaturated monomer derived from monoene according to the olefin copolymer (composition VII) of other composition of additive of the present invention, or can indirectly prepare by the polymkeric substance of hydrogenation derived from many unsaturated monomers such as isoprene or divinyl.Except ethene, preferred multipolymer comprises derived from the alpha-olefin with 3 to 24 carbon atoms and has the structural unit that molecular weight is up to 120 000g/mol.Preferred alpha-olefin is propylene, butylene, iso-butylene, n-hexylene, dissident's alkene, positive octene, isooctene, positive decene, isodecyl alkene.Co-monomer content with alpha-olefin of 3 to 24 carbon atoms is preferably 15 to 50mol%, and particularly preferably 20 to 35mol% and especially 30 to 45mol%.These multipolymers also can comprise on a small quantity, for example are up to other comonomer of 10mol%, for example nonterminal olefin or non-conjugated alkene.Ethylene-propylene copolymer preferably.Olefin copolymer can be by known method, for example utilizes Ziegler or metallocene catalyst and prepares.

Further suitable olefin copolymer is to comprise the block that is made of the unsaturated aromatic monomer A of olefinic and the segmented copolymer of the block that is made of hydrogenation polyolefine B.Especially suitable is to have structure (AB) _nA and (AB) _mSegmented copolymer, wherein n is that 1 to 10 number and m are 2 to 10 numbers.

The additive combination of the present invention that is comprised of I and II is as a side and other composition V, and VI and VII generally are 1: 10 to 10: 1 as the opposing party's mixture ratio in each case, are preferably 1: 5 to 5: 1.

This additive can use separately or with other additive, for example with other pour point depressant or dewaxing agent, with antioxidant, cetane number improver, de-misting agent, emulsion splitter, washing composition, dispersion agent, defoamer, dyestuff, inhibiter, oiliness additive, mud inhibitor, odorant and/or use together for reducing the additive of cloud point.

Additive of the present invention increases mineral oil fractions such as gasoline, kerosene, jet fuel, the specific conductivity of diesel oil and oil fuel, wherein they are lower than 21 % by weight having, especially be lower than 19 % by weight, particularly be lower than 18 % by weight, for example be lower than in the oil of low aromatic content of 17 % by weight advantageous particularly.Because they improve especially mineral oil fractions such as kerosene simultaneously, jet fuel, the cold flow performance of diesel oil and oil fuel, thus can realize obviously saving total additive capacity of oil by their use, because needn't add additional specific conductivity improving agent.In addition, therein since weather condition and do not use so far cold additive the zone or the time, the for example cloud point of the oil of additive to be added and/or CFPP can by be blended into be rich in paraffin, not too expensive mineral oil fraction is adjusted to higher level, this has improved the economy of refinery.Additive of the present invention does not comprise metal in addition, it may produce ash and therefore be created in the settling in combustion chamber or the waste gas system and cause surrounding environment when burning particle load.

At this, the specific conductivity that adds the oil of additive according to the present invention does not reduce with drop in temperature, and in many cases even observe by the unknown specific conductivity that occurs with drop in temperature of prior art additive and increase, guarantee like this even the safety operation under low ambient temperature.Another advantage of additive of the present invention is, this adds the oil of additive even at longer-term, keeps specific conductivity in namely between the shelf liveves in several weeks.In addition, in according to proper mixture ratio rate scope of the present invention, do not occur uncompatibility between composition I and the II, they are opposite with the additive of US 4 356 002 like this, can be formulated as the enriched material form no problemly.

They are particularly useful for improving the refining of having experienced under hydrogenation conditions and only hang down mineral oil fractions such as the jet fuel many aromatics of ratio and compound polarity, gasoline, kerosene, the antistatic property of diesel oil and oil fuel to reduce sulphur content and therefore to comprise.Additive of the present invention is lower than 350ppm sulphur comprising, and particularly preferably is lower than 100ppm sulphur, especially is lower than 50ppm sulphur, and under special circumstances, is lower than in the mineral oil fractions of 10ppm sulphur advantageous particularly.These oily water-contents are lower than 150ppm, are lower than in some cases 100ppm, for example are lower than 80ppm.These oily specific conductivity are usually less than 10pS/m and often even be lower than 5pS/m.

Especially preferred mineral oil fractions is middle runnings.Middle runnings refers in particular to those mineral oil that obtain and seethe with excitement by distilling the crude oil, for example kerosene, jet fuel, diesel oil and oil fuel under 120 to 450 ℃.Their preferred sulphur, aromatic substance and water-content as above illustrate.The present composition is lower than 360 ℃ having, especially 350 ℃ and be lower than under special circumstances in 90% those middle runningss that distillate a little of 340 ℃ advantageous particularly.Aromatic substance refer to by single-, two-and the summation that forms of polynuclear aromatic compound, for example it can utilize HPLC to measure according to DIN EN 12916 (2001 editions).Middle runnings also can comprise minor amount, for example is up to 40 volume %, preferred 1 to 20 volume %, especially 2 to 15 volume %, for example animal and/or the oil of plant origin, for example fatty acid methyl ester hereinafter described in detail of 3 to 10 volume %.

The present composition is equally applicable to improve the antistatic property of the motor spirit (biological motor spirit) based on renewable raw materials.Biological motor spirit refer to can be used as motor spirit and especially as diesel oil or oil fuel by animal material and preferred by vegetable material or oil that both obtain, with and derivative.They refer in particular to the triglyceride level of the lipid acid with 10 to 24 carbon atoms, and can be by its lower alcohol that obtains by transesterification reaction such as the fatty acid ester of methyl alcohol or ethanol.

The example of suitable biological motor spirit is rapeseed oil, Fructus Coriandri oil, soybean oil, Oleum Gossypii semen, sunflower oil, Viscotrol C, sweet oil, peanut oil, Semen Maydis oil, Prunus amygdalus oil, palm-kernel oil, Oleum Cocois, canola, butter, animal oil, fish oil and with the edible oil of crossing.Other example comprises derived from wheat, jute, sesame, Butyrospermum Parkii nut, the oil of peanut oil and Toenol 1140.The fatty acid alkyl ester that is also referred to as biofuel can be by method well known in the prior art derived from these oil.Rapeseed oil preferably, it is the mixture with the lipid acid of glycerine esterification, because it can obtain in a large number and can be in a simple manner by squeezing out of Semen Brassicae campestris obtained.In addition, the preferably same Sunflower Receptacle that extensively distributes and the oil of soybean, with and with the mixture of rapeseed oil.

It is especially applicable that what make biological motor spirit is the lower alkyl esters of lipid acid.Applicable at this is for example, to have the lipid acid of 14 to 22 carbon atoms, lauric acid for example, tetradecanoic acid, palmitinic acid, Zoomeric acid, stearic acid, oleic acid, elaidic acid, petroselinic acid, ricinolic acid, eleostearic acid, linolic acid, linolenic acid, arachic acid, cis 9-eicosenoic acid, the ethyl ester of docosoic acid or erucic acid, propyl ester, butyl ester and the commercial mixture of methyl esters especially.It is 50 to 150 and especially 90 to 125 that preferred ester has iodine number.Mixture with especially favourable performance is mainly to comprise, and namely comprises those of methyl esters of the lipid acid with the two keys of 16 to 22 carbon atoms and 1,2 or 3 of at least 50 % by weight.Preferred fatty acid lower alkyl esters is the methyl esters of oleic acid, linolic acid, linolenic acid and erucic acid.

Additive of the present invention is equally applicable to improve the antistatic property of turbine engine fuel.These are at approximately 65 ℃ of boilings and for example with name of an article JP-4 to about 330 ℃ the temperature range, JP-5, JP-7, JP-8, the motor spirit that Jet A and Jet A-1 sell.JP-4 and JP-5 stipulate in MIL Specifications MIL-T-5624-N and JP-8 stipulates in MIL Specifications MIL-T-83133-D; Jet A, Jet A-1 and Jet B stipulate in ASTM D1655.

Additive of the present invention is equally applicable to improve as solvent, for example, is used for the textiles cleaning or for the production of the specific conductivity of the hydrocarbon of paint and coating.

Embodiment

Table 1: the sign of test oil:

Used test oil is the oil that derives from European refinery.The CFPP value measures according to EN 116 and cloud point is measured according to ISO 3015.Aromatic hydrocarbon radical is measured according to DIN EN 12916 (version in November calendar year 2001).

	Test oil 1	Test oil 2	3 (contrasts) of test oil
				Distill IBP[℃] 20%[℃] 90%[℃] FBP[℃]	212 244 322 342	188 249 336 361	160 229 339 371
Cloud point [℃]	-8.8	-12.5	4.6
				15 ℃ of [g/cm of density@ ³]	0.8302	0.8264	0.8410
20 ℃ of water-content@[ppm]	25	35	185
				Sulphur content [ppm]	4	6	173
25 ℃ of specific conductivity@[pS/m]	0	1	9
				Single [wt%] two [wt%] many [wt%] of aromatic content [wt%]	14.8 14.5 0.3 ＜0.1	16.9 14.4 2.4 0.1	29.9 24.1 5.3 0.5

Use following additive:

(A) sign of used alkyl phenol resin

A1	Acid catalysed nonyl benzene resinox (Mw 1300g/mol)
		A2	Acid catalysed nonyl benzene resinox (Mw 2200g/mol)
A3	Acid catalysed dodecyl phenol-formaldehyde resin (Mw 2600g/mol)
		A4	Dodecyl phenol-the formaldehyde resin of base catalysis (Mw 2450g/mol)
A5	Under acidic catalyst by the alkyl resinox (Mw 2900g/mol) of the nonylphenol of equimolar ratio example and butylphenol preparation
		A6	According to the oxyalkylated nonylphenol resin (contrast) of A2 with 5mol ethylene oxide/phenols OH group

Molecular weight utilizes gel permeation chromatography to measure with respect to the PEG standard substance in THF.Resin A 1) to A4) use with 50% instrumentality in solvent naphtha (a kind of commercial mixture of high boiling point aromatic hydrocarbon).

(B) sign of used nitrogenous compound B

B1	According to methacrylic acid-N of EP 0909305, N, N-(trimethyl ammonium) ethyl ester and ethyl acrylate be according to 1: 4 multipolymer of mol ratio, 20 % concentration in the higher aromatic solvent.
		B2	Ethene, the terpolymer of 17 % by weight vinyl-acetic esters and 8 % by weight l-vinyl-2-pyrrolidones, the melt viscosity under 140 ℃ is 170mPas, 50% concentration in the higher aromatic solvent.
B3	Ethene, the quaternised terpolymer of usefulness sulfuric acid dimethyl esters of 14 % by weight propionate and 10 % by weight dimethylaminoethyl acrylate methyl base amino-ethyl esters, melt viscosity 220 mPas under 140 ℃, 50% concentration in the higher aromatic solvent.
		B4	N-butter fatty alkyl-1, the multipolymer of 3-propylene diamine and Epicholorohydrin, 30% concentration in aromatic solvent

Improvement to the specific conductivity of middle cut

In order to measure specific conductivity, the additive that will have given in each case concentration is dissolved under vibration in the 250ml test oil 1.According to DIN 51412-T02-79, use surely wherein specific conductivity of MaihakSLA 900 automatic electric conductance instrumentations.The unit of specific conductivity is slight siemens (Picosiemens)/m (pS/m).For jet fuel, general provision is the specific conductivity of 50pS/m at least.Given metering is than the amount based on used active substance.

Table 2: the specific conductivity in the test oil 1

Table 3: the specific conductivity in the test oil 2

Table 4: the specific conductivity (contrast) in the test oil 3

Embodiment shows, the present composition is compared with single component has obvious synergy.They show in addition, and the present composition is compared the specific conductivity that has increased the low aromatic oil fuel that especially has low water content at higher degree with known prior art additive.The specific conductivity that adds the mineral oil fractions of additive according to the present invention raises along with drop in temperature.Because used additive also improves other performance of middle runnings in addition, for example paraffin dissemination and oilness are so can realize comparable specific conductivity under the low additive dosage of conventional additives.Another advantage of the present invention is, except improving specific conductivity, uses additive of the present invention to improve simultaneously low-temperature performance, and this allows the manufacturers of oil fuel can process the problematic distillation fraction that is rich in paraffin under cold condition of higher proportion.

Claims

1. mineral oil fractions, its water-content is 50pS/m at least for being lower than 150ppm and specific conductivity, and this mineral oil fractions comprises 0.1 to 200ppm at least a alkylphenol-aldehyde resins and 0.1 to 200ppm at least a polymer with nitrogen, and this polymer with nitrogen is selected from:

A) by having C ₄-to C ₄₀The comb-shaped polymer of the direct copolymerization preparation of the monomer of-alkyl group and at least a nitrogenous comonomer, wherein said have a C ₄-to C ₄₀The monomer of-alkyl group is selected from C ₄-to C ₄₀The ester of the oil soluble ethylenically unsaturated carboxylic acids of-alkyl group, oil-soluble ethylene base ester, oil-soluble ethylene base ether or have the alkene of 6 to 42 carbon atoms;

C) the polymer-type polyamines by aliphatic series uncle's monoamine or N-alkylenediamines and Epicholorohydrin or Racemic glycidol condensation are prepared,

Wherein said at least a alkylphenol-aldehyde resins comprises the repeated structural unit of following formula

R wherein ⁵C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, O-R ⁶Or O-C (O)-R ⁶, R ⁶C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, and n is 2 to 100 number.

2. the mineral oil fractions of claim 1, the alkyl group of wherein said at least a alkylphenol-aldehyde resins comprises 1 to 200 carbon atom.

3. the mineral oil fractions of claim 1, the molecular weight of wherein said at least a alkylphenol-aldehyde resins are 400 to 20000g/mol.

4. the mineral oil fractions of claim 1, wherein said at least a polymer with nitrogen also comprises 0.1 to 15mol% and is selected from the unsaturated nitrogenous comonomer of following olefinic except comprising ethene:

I) alkyl amido acrylate or alkylamino methacrylic ester,

Ii) alkyl acrylamide and alkyl methyl acrylamide,

Iii) vinylamide,

Iv) aminoalkyl group vinyl ether,

V) the olefinic unsaturated amine and/or

Vi) with the heterocycle of vinyl groups.

5. the mineral oil fractions of claim 1, wherein said at least a polymer with nitrogen is polyamines, this polyamines is that its alkyl group has the primary alkyl amine of 8 to 24 carbon atoms or its alkyl group and has the N-alkylenediamines that 8 to 24 carbon atoms and its alkylidene group have 2 to 6 carbon atoms, with Epicholorohydrin or Racemic glycidol be 2 to 20 condensation product according to the condensation degree that has of mol ratio 1: 1 to 1: 1.5.

6. the mineral oil fractions of claim 1 wherein additionally comprises the multipolymer that is formed by ethene and 6 to 21mol% vinyl ester, acrylate, methacrylic ester, alkyl vinyl ether and/or alkene.

7. the mineral oil fractions of claim 1 wherein additionally comprises the following formula comb-shaped polymer

Wherein

A is R ', COOR ', OCOR ', R " COOR ', OR ';

D is H, CH ₃, A or R ";

E is H, A;

G is H, R ", R " COOR ', aromatic yl group or heterocyclic group;

M is H, COOR ", OCOR ", OR " and, COOH;

N is H, R ", COOR ", OCOR " and, aromatic yl group;

R ' is the hydrocarbon chain with 8 to 50 carbon atoms;

R " is the hydrocarbon chain with 1 to 10 carbon atom;

M is 0.4 to 1.0 number; With

N is 0 to 0.6 number.

8. the mineral oil fractions of claim 1 wherein additionally comprises the poly (oxyalkylene) based compound, and described compound is selected from ester, ether and ether/ester, and has the alkyl group of 12 to 30 carbon atoms with at least one.

9. the mineral oil fractions of claim 1 wherein additionally comprises and has the multipolymer that molecular weight is up to 120000g/mol, and this multipolymer also comprises the structural unit derived from the alpha-olefin with 3 to 24 carbon atoms except comprising the ethene structural unit.

10. the mineral oil fractions of claim 1 wherein additionally comprises the polysulfones derived from the alkene with 6 to 20 carbon atoms.

11. the mineral oil fractions of claim 1 wherein additionally comprises paraffin dispersant, it is aliphatic amide and the reaction product that comprises the compound of at least one carboxyl groups, and wherein said aliphatic amide is formula NR ⁶R ⁷R ⁸Compound, R wherein ⁶, R ⁷And R ⁸Be identical or different, and at least one is C in these groups ₈-C ₃₆-alkyl, C ₆-C ₃₆-cycloalkyl or C ₈-C ₃₆-alkenyl, and remaining group is hydrogen, C ₁-C ₃₆-alkyl, C ₂-C ₃₆-alkenyl, cyclohexyl, or formula-(CH ₂) _nThe group of-NYZ, wherein n=2,3 or 4, and Y and Z are H or C independently of one another ₁-C ₃₀-alkyl.

12. the mineral oil fractions of claim 11, wherein R ⁶, R ⁷And R ⁸In at least one is C ₁₂-C ₂₄-alkyl, C ₁₂-C ₂₄-alkenyl or cyclohexyl.

13. one kind is improved the method for specific conductivity that water-content is lower than the mineral oil fractions of 150ppm, it carries out in the following way: add the composition that comprises at least a alkylphenol-aldehyde resins and count 0.1 to 10 at least a polymer with nitrogen of weight part based on described alkylphenol-aldehyde resins in described mineral oil fractions, this polymer with nitrogen is selected from

So that having specific conductivity, mineral oil fractions is 50pS/m at least,

14. one kind is improved the method for specific conductivity that water-content is lower than the mineral oil fractions that comprises 0.1 to 200ppm at least a polymer with nitrogen of 150ppm, this polymer with nitrogen is selected from

It carries out in the following way: adds 0.1 to 200ppm at least a alkylphenol-aldehyde resins in the described mineral oil fractions, is 50pS/m at least so that described mineral oil fractions has specific conductivity,

R wherein ⁵C ₁-C ₂₀₀Alkyl or C ₂-C ₂₀₀-alkenyl, O-R ⁶Or O-C (O)-R ⁶, R ⁶C ₁-C ₂₀₀-alkyl or C ₂-C ₂₀₀-alkenyl, and n is 2 to 100 number.

15. one kind is used for the additive that water-content is lower than the mineral oil fractions of 150ppm, it comprises mass ratio is 9: 1 to 1: 9 at least a alkylphenol-aldehyde resins and at least aly is selected from following polymer with nitrogen:

And composition thereof,